Primary Site >> Esophagus Cancer
Gene >> TNFRSF18
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000379268 |
| Start | 1203884:1203884(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs763921252 |
| CDS Mutation | c.686C>T |
| AA Mutation | p.Ser229Leu(p.S229L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |